Variant report

Variant	rs73060760
Chromosome Location	chr3:179658851-179658852
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11708154	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11709733	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11718907	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1404271	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1599791	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16830940	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17691911	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17748709	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17748864	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2302741	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2302742	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28619517	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs41265425	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4146789	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56263652	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56395499	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56677569	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56836862	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57376419	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57823511	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs59018122	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs59453720	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73058681	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73060731	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73060761	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73060768	0.87[AFR][1000 genomes]
rs7630877	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7637613	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7646149	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9290685	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs940523	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9682757	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9831383	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9836757	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179644400-179660000	Weak transcription	Pancreas	Pancrea
2	chr3:179648400-179660000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:179652000-179660200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:179653000-179659200	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:179653600-179660400	Weak transcription	Brain Substantia Nigra	brain
6	chr3:179654000-179659800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:179656600-179664200	Strong transcription	Dnd41	blood
8	chr3:179657400-179660000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr3:179657600-179659800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr3:179657800-179659800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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